Half-Metallicity in Pb2CoReO6 Double Perovskite and High Magnetic Ordering Temperature in Pb2CrReO6 Perovskite

نویسندگان

  • Maria Retuerto
  • Man-Rong Li
  • Peter W. Stephens
  • Javier Sańchez-Benítez
  • Xiaoyu Deng
  • Gabriel Kotliar
  • Mark C. Croft
  • Alexander Ignatov
  • David Walker
  • Martha Greenblatt
چکیده

Pb2MReO6 (M = Co, Cr) perovskites were prepared by high pressure−high temperature method. Rietveld refinements of synchrotron powder X-ray diffraction show that the crystal structure of Pb2CoReO6 is trigonal (space group R-3) with almost complete ordering of Co and Re cations, while Pb2CrReO6 (space group Pm-3m) is a cubic perovskite with one single site for Cr and Re atoms. The difference between the symmetry and the degree of order was further clarified by X-ray absorption spectroscopy that establishes formal oxidation states in these phases as Pb2Co ReO6 and Pb2Cr ReO6. Pb2CrReO6 is a simple perovskite with a high magnetic ordering temperature of 643 K. Pb2CoReO6 is a double perovskite with −23% high field negative magnetoresistance at 10 K and 9 T. First-principles calculations of Pb2CoReO6 indicate a half metallic electronic structure.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Magnetoresistance in ordered and disordered double perovskite oxide, Sr2FeMoO6

We have prepared crystallographically ordered and disorder specimens of the double perovskite, Sr2FeMoO6 and investigated their magnetoresistance behaviour. The extent of ordering between the Fe and Mo sites in the two samples is determined by Rietveld analysis of powder x-ray diffraction patterns and reconfirmed by Mössbauer studies. While the ordered sample exhibits the sharp low-field respon...

متن کامل

Complex magnetic behaviour of Sr2CoNb1-xTixO6 (0 ≤ x ≤ 0.5) as a result of a flexible microstructure.

We report the rich magnetic behaviour of Sr2CoNb1-xTixO6 (0 ≤ x ≤ 0.5) oxides as a result of their complex microstructure. Although these oxides show an average simple-cubic perovskite structure, they present a flexible microstructure due to short-range ordering between Co/Ti and Nb cations in the perovskite B-sites. The microstructure consists of double-cubic perovskite domains grown in a simp...

متن کامل

Structural, Magnetic and Catalytic Properties of Non-Stoichiometric Lanthanum Ferrite Nano-Perovskites in Carbon Monoxide Oxidation

Perovskite-type oxides of LaFe(1+x)O(3+δ) (x = 0.0, 0.2, 0.5 and 0.7) were synthesized by citrate sol–gel methodto ensure the formation of nanosized perovskites. The physicochemical properties of these LaFe(1+x)O(3+δ)materials were characterized by thermal gravimetric/differential analyses, Fourier transform infraredspectroscopy, X-ray powder diffraction, scanning electron and...

متن کامل

Two-dimensional ferromagnetic ordering and magnetoresistance in the layered perovskite La222xCa112xMn2O7

The resistivity and magnetization of layered perovskite La222xCa112xMn2O7 have been studied systematically using bulk samples with a wide doping concentration range 0<x<0.5 and epitaxial thin film samples with x50.3. The system becomes a metallic ferromagnet for doping concentrations 0.22<x<0.5. In this doping region, results for bulk samples as well as for thin films have clearly shown that th...

متن کامل

EPR and Magnetic Properties of the CanFe2Mnn-2O3n-1 Perovskite Related Series

We present EPR and Susceptibility measurements performed on the perovskite-like family CanFe21vln,,20,,,. On going from n=2 to n=3 Fe3+ is progressively replaced by Mne. As a consequence the ordering temperature is depressed and frustrations in the magnetic interactions were found. The measurements are compared with the previously studied system CanFe2Ti,i,203n-, where magnetic Mn4+ were replac...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2015